A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569927



Internal ID16010650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094008..72095652hg38UCSC Ensembl
Innerchr15:72386349..72387993hg19UCSC Ensembl
Innerchr15:70173403..70175047hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381645
hg191645
hg181645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4613n54
Supporting Variantsnssv845000, nssv844997, nssv845001, nssv844998, nssv844996, nssv845002, nssv844999
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569927
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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